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A national consensus management pathway for paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS): results of a national Delphi process.
Harwood, Rachel; Allin, Benjamin; Jones, Christine E; Whittaker, Elizabeth; Ramnarayan, Padmanabhan; Ramanan, Athimalaipet V; Kaleem, Musa; Tulloh, Robert; Peters, Mark J; Almond, Sarah; Davis, Peter J; Levin, Michael; Tometzki, Andrew; Faust, Saul N; Knight, Marian; Kenny, Simon.
  • Harwood R; Department of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK. Electronic address: Rachel.Harwood@liverpool.ac.uk.
  • Allin B; National Perinatal Epidemiology Unit, Nuffield Department of Health, University of Oxford, Oxford, UK; Department of Paediatric Surgery, Ozxford Children's Hospital, Oxford, UK.
  • Jones CE; NIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton Foundation NHS Trust and Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, UK.
  • Whittaker E; Department of Paediatrics, Imperial College Healthcare NHS Trust, London, UK; Section of Paediatric Infectious Disease, Department of Infectious Disease, Imperial College London, London, UK.
  • Ramnarayan P; Children's Acute Transport Service, Great Ormond Street Hospital for Children, London, UK.
  • Ramanan AV; Department of Paediatric Rheumatology, Bristol Royal Hospital for Children, Bristol, UK; Royal National Hospital for Rheumatic Diseases, Bath, UK; University of Bristol, Bristol, UK.
  • Kaleem M; Department of Paediatric Radiology, Alder Hey Children's Hospital, Liverpool, UK.
  • Tulloh R; Department of Paediatric Cardiology, Bristol Royal Hospital for Children, Bristol, UK; University of Bristol, Bristol, UK.
  • Peters MJ; University College London Great Ormond Street Institute of Child Health and Great Ormond Street Hospital NHS Trust, NIHR Biomedical Research Centre, London, UK.
  • Almond S; Department of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK.
  • Davis PJ; Paediatric Intensive Care Unit, Bristol Royal Hospital for Children, Bristol, UK.
  • Levin M; Department of Paediatrics, Imperial College Healthcare NHS Trust, London, UK; Section of Paediatric Infectious Disease, Department of Infectious Disease, Imperial College London, London, UK.
  • Tometzki A; Department of Paediatric Cardiology, Bristol Royal Hospital for Children, Bristol, UK.
  • Faust SN; NIHR Southampton Clinical Research Facility and Biomedical Research Centre, University Hospital Southampton Foundation NHS Trust and Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, UK.
  • Knight M; National Perinatal Epidemiology Unit, Nuffield Department of Health, University of Oxford, Oxford, UK.
  • Kenny S; Department of Paediatric Surgery, Alder Hey Children's Hospital, Liverpool, UK; School of Life Sciences, University of Liverpool, Liverpool, UK; NHS England/Improvement, Redditch, UK.
Lancet Child Adolesc Health ; 5(2): 133-141, 2021 02.
Article in English | MEDLINE | ID: covidwho-779849
ABSTRACT
Paediatric inflammatory multisystem syndrome temporally associated with COVID-19 (PIMS-TS) is a novel condition that was first reported in April, 2020. We aimed to develop a national consensus management pathway for the UK to provide guidance for clinicians caring for children with PIMS-TS. A three-phase online Delphi process and virtual consensus meeting sought consensus over the investigation, management, and research priorities from multidisciplinary clinicians caring for children with PIMS-TS. We used 140 consensus statements to derive a consensus management pathway that describes the initial investigation of children with suspected PIMS-TS, including blood markers to help determine the severity of disease, an echocardiogram, and a viral and septic screen to exclude other infectious causes of illness. The importance of a multidisciplinary team in decision making for children with PIMS-TS is highlighted throughout the guidance, along with the recommended treatment options, including supportive care, intravenous immunoglobulin, methylprednisolone, and biological therapies. These include IL-1 antagonists (eg, anakinra), IL-6 receptor blockers (eg, tocilizumab), and anti-TNF agents (eg, infliximab) for children with Kawasaki disease-like phenotype and non-specific presentations. Use of a rapid online Delphi process has made it possible to generate a national consensus pathway in a timely and cost-efficient manner in the middle of a global pandemic. The consensus statements represent the views of UK clinicians and are applicable to children in the UK suspected of having PIMS-TS. Future evidence will inform updates to this guidance, which in the interim provides a solid framework to support clinicians caring for children with PIMS-TS. This process has directly informed new PIMS-TS specific treatment groups as part of the adaptive UK RECOVERY trial protocol, which is the first formal randomised controlled trial of therapies for PIMS-TS globally.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / Critical Pathways / Disease Management / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Child / Humans Country/Region as subject: Europa Language: English Journal: Lancet Child Adolesc Health Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Systemic Inflammatory Response Syndrome / Critical Pathways / Disease Management / COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Limits: Child / Humans Country/Region as subject: Europa Language: English Journal: Lancet Child Adolesc Health Year: 2021 Document Type: Article